510(k) K885000 ยท LOS
Q750 ELECTROCARDIOGRAPH
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Feb 23, 1989 |
| Received | Dec 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885000
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.